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VRV-II Vacuum Relief Valve

FDA UDI

Class II (US FDA UDI)

by Quest Medical Inc

Identity

Trade Name
VRV-II Vacuum Relief Valve FDA UDI
Generic Name
Cardiopulmonary bypass system valve, unidirectional flow/pressure control FDA UDI
Device Name
Bulk, non-sterile VRV-II Vacuum Relief Valve. Contains 50 non-sterile valves. The sterile version is Model 4003103. FDA UDI
Model / Reference
4003203 FDA UDI
Description
Bulk, non-sterile VRV-II Vacuum Relief Valve. Contains 50 non-sterile valves. The sterile version is Model 4003103. FDA UDI

Identifiers

Primary DI / UDI-DI
10634624432038 FDA UDI
FDA Product Code
DWD FDA UDI
GMDN Term
Cardiopulmonary bypass system valve, unidirectional flow/pressure control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Cardiopulmonary bypass system valve, unidirectional flow/pressure control

VRV-II Vacuum Relief Valve by Quest Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system valve, unidirectional flow/pressure control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quest Medical Inc

Sources (1)

  • FDA UDI f30c8df8-b169-435d-8f6c-c8b126880596 33 fields · synced Jun 8, 2026